Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2302685
BCL2L14 ; LRP6
0.827 0.240 12 12148964 missense variant C/T snv 0.85 0.84 5
rs150599989
C5AR2
0.827 0.320 19 47341767 missense variant G/A;C;T snv 4.0E-06; 9.6E-05 5
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs121964971
CBS
0.851 0.160 21 43058215 missense variant G/A snv 1.2E-05 5
rs2811712
CDKN2B-AS1
0.882 0.080 9 21998036 intron variant G/A snv 0.85 5
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1251035592
CYP3A5 ; ZSCAN25
1.000 0.040 7 99664039 missense variant T/C snv 4.2E-06 1
rs8450
DENND4B ; CRTC2
1.000 0.040 1 153947810 3 prime UTR variant G/A snv 0.27 2
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs200960801
ESR1
0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1256049
ESR2
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs920435389
FGFR4
1.000 0.040 5 177091064 missense variant G/C snv 3
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs498005
HCN4
0.851 0.160 15 73327969 intron variant C/T snv 0.48 5
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs2854744
IGFBP3
0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs886916693
KIDINS220
1.000 0.040 2 8806360 missense variant T/C snv 4.1E-06 1
rs879254840
LDLR ; MIR6886
0.827 0.120 19 11113322 missense variant A/G snv 5